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Shafika Al-Awadi

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Kuwait

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TOP 3
M Afzal; S Oommen; Shafika A Al-Awadi
Transformation of chenodeoxycholic acid by thermophilic Geobacillus stearothermophilus.
JM al-Hassan; Abdulaziz Alkhamis; S Oommen; Shafika A Al-Awadi; M Afzal
Tryptophan oxidative metabolism catalyzed by geobacillus stearothermophilus: a thermophile isolated from kuwait soil contaminated with petroleum hydrocarbons.
Safa Al-Tamimi; Shafika A Al-Awadi; S Oommen; M Afzal
Modification of progesterone and testosterone by a food-borne thermophile Geobacillus kaustophilus.

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All Publications

2011: M Afzal; S Oommen; Shafika A Al-Awadi
Transformation of chenodeoxycholic acid by thermophilic Geobacillus stearothermophilus.
Biotechnology and applied biochemistry 2011;58(4):250-5.
2011: JM al-Hassan; Abdulaziz Alkhamis; S Oommen; Shafika A Al-Awadi; M Afzal
Tryptophan oxidative metabolism catalyzed by geobacillus stearothermophilus: a thermophile isolated from kuwait soil contaminated with petroleum hydrocarbons.
International journal of tryptophan research : IJTR 2011;4():1-6.
2010: Safa Al-Tamimi; Shafika A Al-Awadi; S Oommen; M Afzal
Modification of progesterone and testosterone by a food-borne thermophile Geobacillus kaustophilus.
International journal of food sciences and nutrition 2010;61(1):78-86.
2009: Makia J Marafie; Shafika A Al-Awadi; Fatemah Al-Mosawi; Alaa Elshafey; Waleed Al-Ali; Fahd Al-Mulla
Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing.
Familial cancer 2009;8(4):289-98.
2006: Abdel W Awadalla; Jude U Ohaeri; Adel M Tawfiq; Shafika A Al-Awadi
Subjective quality of life of outpatients with diabetes: comparison with family caregivers' impressions and control group.
Journal of the National Medical Association 2006;98(5):737-45.
2006: Abdel W Awadalla; Jude U Ohaeri; Shafika A Al-Awadi; Adel M Tawfiq
Diabetes mellitus patients' family caregivers' subjective quality of life.
Journal of the National Medical Association 2006;98(5):727-36.
2006: Suad Alfadhli; Abdulmutalib Behbehani; Alaa Elshafey; Sidky Abdelmoaty; Shafika A Al-Awadi
Molecular and clinical evaluation of primary congenital glaucoma in Kuwait.
American journal of ophthalmology 2006;141(3):512-6.
2005: S A Madi; RL al-Naggar; Shafika A Al-Awadi; Layla Bastaki
Profile of major congenital malformations in neonates in Al-Jahra region of Kuwait.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-ṣiḥḥīyah li-sharq al-mutawassiṭ 2005;11(4):700-6.
2005: SM Tayel; M M Fawzia; Niran A Al-Naqeeb; Said Gouda; Shafika A Al-Awadi; Kamal Naguib
A morpho-etiological description of congenital limb anomalies.
Annals of Saudi medicine 2005;25(3):219-27.
2005: Shafika A Al-Awadi; M Afzal; S Oommen
Studies on Bacillus stearothermophilus. Part IV. Influence of enhancers on biotransformation of testosterone.
Steroids 2005;70(4):327-33.
2004: Suad Alfadhli; Matra Salim; Shafika A Al-Awadi
A novel germline mutation in the von Hippel-Lindau gene in patients in Kuwait.
Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2004;13(6):312-5.
2004: Suad Alfadhli; Alaa Elshafey; Layla Bastaki; Shafika A Al-Awadi
CTG repeat number at the myotonic dystrophy locus in healthy Kuwaiti individuals: possible explanation of why myotonic dystrophy is rare in Kuwait.
Archives of neurology 2004;61(6):895-8.
2003: Shafika A Al-Awadi; M Afzal; S Oommen
Studies on Bacillus stearothermophilus. Part III. Transformation of testosterone.
Applied microbiology and biotechnology 2003;62(1):48-52.
2002: Shafika A Al-Awadi; M Afzal; S Oommen
Studies on Bacillus stearothermophilus. Part II. Transformation of progesterone.
The Journal of steroid biochemistry and molecular biology 2002;82(2-3):251-6.
2001: Shafika A Al-Awadi; M Afzal; S Oommen
Studies on Bacillus stearothermophilus. Part 1. Transformation of progesterone to a new metabolite 9,10-seco-4-pregnene-3,9,20-trione.
The Journal of steroid biochemistry and molecular biology 2001;78(5):493-8.
1999: Kamal Naguib; Shafika A Al-Awadi; M A A Moussa; Layla Bastaki; Said Gouda; M A Redha; F Mustafa; SM Tayel; S A Abulhassan; D S Murthy
Trisomy 18 in Kuwait.
International journal of epidemiology 1999;28(4):711-6.
1999: Kamal Naguib; Shafika A Al-Awadi; Layla Bastaki; M A A Moussa; S A Abulhassan; SM Tayel; K Murthy
Clustering of trisomy 18 in Kuwait: Genetic predisposition or environmental?
Annals of Saudi medicine 1999;19(3):197-200.
1999: S J Abulhasan; SM Tayel; Shafika A Al-Awadi
Mosaic Turner syndrome: cytogenetics versus FISH.
Annals of human genetics 1999;63(Pt 3):199-206.
1999: SM Tayel; RL al-Naggar; D S Krishna Murthy; Kamal Naguib; Shafika A Al-Awadi
Familial pericentric inversion of chromosome 1 (p36.3q23) and Bardet-Biedl syndrome.
Journal of medical genetics 1999;36(5):418-9.
1999: M A Mubashir; Mohamed A Sabry; SA Farah; N Haseeb; B Quasrawi; Waleed A Al-Busairi; R al-Dabbous; Shafika A Al-Awadi; TI Farag
New syndromic entity of situs inversus totalis.
Clinical dysmorphology 1999;8(1):23-7.
1999: Mohamed A Sabry; TI Farag; AA Shaltout; Mohamed Zaki; Z Al-Mazidi; SJ Abulhassan; NA al-Torki; A Quishawi; Shafika A Al-Awadi
Kenny-Caffey syndrome: an Arab variant?
Clinical genetics 1999;55(1):44-9.
1998: SM Tayel; Mohamed A Sabry; N A Kader; SA Farah; Shafika A Al-Awadi; TI Farag
Triophthalmia and facial clefting: a case report.
Journal of medical genetics 1998;35(10):875-7.
1998: NA al-Torki; Mohamed A Sabry; A Al-Tawari; N H Al-Kandari; Shafika A Al-Awadi
Craniofacial dyssynostosis with cryptorchidism and normal stature.
American journal of medical genetics 1998;79(1):5-7.
1998: SA Farah; TI Farag; Mohamed A Sabry; ST Simeonov; S al-Khattam; SJ Abulhassan; B Quasrawi; Waleed A Al-Busairi; Shafika A Al-Awadi
Cutis verticis gyrata-mental deficiency syndrome: report of a case with unusual neuroradiological findings.
Clinical dysmorphology 1998;7(2):131-4.
1998: R al-Dabbous; Mohamed A Sabry; SA Farah; Shafika A Al-Awadi; ST Simeonov; TI Farag
The autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease: report of another Bedouin family.
Clinical dysmorphology 1998;7(2):127-30.
1998: Mohamed A Sabry; Mohamed Zaki; S J Abul Hassan; Dina Ramadan; M A Abdel Rasool; Shafika A Al-Awadi; Qusay Al-Saleh
Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster.
Journal of medical genetics 1998;35(1):31-6.
1997: NA al-Torki; Mohamed A Sabry; Shafika A Al-Awadi; N Al-Tarkeit
Lowry-Maclean syndrome with osteopenic bones and possible autosomal dominant inheritance in a Bedouin family.
American journal of medical genetics 1997;73(4):491-2.
1997: SA Farah; Mohamed A Sabry; Adnan J Khuraibet; J T Anim; B Quasrawi; S Al-Khatam; Waleed A Al-Busairi; JM Hussein; R A Khan; Shafika A Al-Awadi
Marinesco-Sjögren syndrome in a Bedouin family.
Acta neurologica Scandinavica 1997;96(6):387-91.
1997: Mohamed A Sabry; Essam A Ismail; RL al-Naggar; NA al-Torki; SA Farah; Shafika A Al-Awadi; D Obenbergerova; Layla Bastaki
Unusual traits associated with Robinow syndrome.
Journal of medical genetics 1997;34(9):736-40.
1997: Mohamed A Sabry; Mohamed Zaki; Shafika A Al-Awadi; Qusay Al-Saleh; M S Mattar
Non-haematological traits associated with congenital dyserythropoietic anaemia type 1: a new entity emerging.
Clinical dysmorphology 1997;6(3):205-12.
1997: K Tahseen; S Khan; R Uma; R Usha; M M Al Ghanem; Shafika A Al-Awadi; TI Farag
Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed.
American journal of medical genetics 1997;69(2):126-32.
1997: Mohamed A Sabry; Qusay Al-Saleh; SA Farah; D Obenbergerova; ST Simeonov; Shafika A Al-Awadi; TI Farag
Another Arab patient with overlap of Váradi-Papp/Opitz trigonocephaly syndromes?
American journal of medical genetics 1997;68(1):54-7.
1997: NA al-Torki; Shafika A Al-Awadi; L Cindro-Heberie; Mohamed A Sabry
Gerodermia osteodysplastica in a Bedouin sibship: further delineation of the syndrome.
Clinical dysmorphology 1997;6(1):51-5.
1996: M J Marafie; S A Temtamy; U Rajaram; Shafika A Al-Awadi; M H el-Badramany; TI Farag
Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
American journal of medical genetics 1996;66(3):261-4.
1996: Mohamed A Sabry; D Obenbergerova; R Al-Sawan; Q A Saleh; SA Farah; Shafika A Al-Awadi; TI Farag
Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: a report of a Bedouin baby.
Journal of medical genetics 1996;33(2):165-7.
1996: M A Redha; D S Krishna Murthy; Shafika A Al-Awadi; I S al-Sulaiman; Mohamed A Sabry; S A el-Bahey; TI Farag
De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
Annales de génétique 1996;39(1):5-9.
1995: Mohamed A Sabry; Qusay Al-Saleh; R al-Saw'an; Shafika A Al-Awadi; TI Farag
Right upper limb bud triplication and polythelia, left sided hemihypertrophy and congenital hip dislocation, facial dysmorphism, congenital heart disease, and scoliosis: disorganisation-like spectrum or patterning gene defect?
Journal of medical genetics 1995;32(7):555-6.
1994: A A Redha; D S Murthy; H Kandil; TI Farag; R Usha; Shafika A Al-Awadi; L A Jeryan; K al-Nagdy; M el-Ghanem
Partial trisomy of short arm of chromosome 8 (46,XY, inv dup (8) (p21-->pter) in a Bedouin child with multiple congenital anomalies and mental retardation.
Indian journal of pediatrics 1994;61(3):301-6.
1994: TI Farag; Layla Bastaki; M Marafie; Shafika A Al-Awadi; J Krsz
Autosomal recessive congenital diaphragmatic defects in the Arabs.
American journal of medical genetics 1994;50(3):300-1.
1993: TI Farag; Shafika A Al-Awadi; M H el-Badramary; M A Aref; B Kasrawi; D S Krishna Murthy; M Y el-Khalifa; G Yadav; M J Marafie; Layla Bastaki
Disease profile of 400 institutionalized mentally retarded patients in Kuwait.
Clinical genetics 1993;44(6):329-34.
1993: TI Farag; Shafika A Al-Awadi; M H el-Badramany; R Usha; M el-Ghanem
Second family with "apple peel" syndrome affecting four siblings: autosomal recessive inheritance confirmed.
American journal of medical genetics 1993;47(1):119-21.
1993: TI Farag; Shafika A Al-Awadi; M J Marafie; Layla Bastaki; D S Murthy; S A al-Othman; F M Mohamed; A A Reda; S J Abul Hasan; M A Reda
Clustering of cri du chat syndrome among the Bedouins.
American journal of medical genetics 1993;46(3):347-8.
1993: TI Farag; Shafika A Al-Awadi; M J Marafie; Layla Bastaki; S A al-Othman; F M Mohammed; I S AlSuliman; D S Murthy
The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review.
Journal of medical genetics 1993;30(1):62-4.
1993: F M Mohammed; D S Krishna Murthy; TI Farag; Shafika A Al-Awadi; S A al-Othman; I Hammad
Familial pericentric inversion of chromosome 13, 46,XX,inv (13)(p13;q11): a new variant.
Annales de génétique 1993;36(3):181-5.
1992: R Usha; R Uma; TI Farag; Y Girish; M M al-Ghanim; K al-Najdi; Shafika A Al-Awadi; M H el-Badramany
Late diagnosis of phenylketonuria in a Bedouin mother.
American journal of medical genetics 1992;44(6):713-5.
1992: G Yadav; TI Farag; Shafika A Al-Awadi; T Sam; M J Marafie; Layla Bastaki; M Y el Khalifa; B Kasrawi; R A Wahba
Aminoacidopathies among institutionalised mentally retarded in Kuwait.
Clinical genetics 1992;42(4):212.
1991: SM Hegab; S M Sheriff; Shafika A Al-Awadi; Kamal Naguib; A Teebi; C I Phillips
Central pulverulent (Coppock) cataracts. A sibship of two Arab females with full-cousin normal parents.
Ophthalmic paediatrics and genetics 1991;12(2):111-4.
1990: K K Naguib; Shafika A Al-Awadi; TI Farag; F M Mohammed
Penile enlargement in 3q23-q25 deletion syndrome.
American journal of medical genetics 1990;36(3):361-2.
1990: E S Mahfouz; M A Issa; TI Farag; Kamal Naguib; Shafika A Al-Awadi; R N Schimke
Persistent Mullerian duct syndrome: report of two boys with associated crossed testicular ectopia.
Journal of pediatric surgery 1990;25(6):692-3.
1990: D S Murthy; T S Sundareshan; TI Farag; Shafika A Al-Awadi; S A al-Othman
Segregation of acrocentric chromosome association in familial dicentric Robertsonian translocation t(14p;22p), aneuploidy (trisomy-21) and heteromorphism.
Indian journal of experimental biology 1990;28(6):511-5.
1990: T S Sundareshan; Kamal Naguib; Shafika A Al-Awadi; M A Redha; M S Hamoud
Apparently nonmosaic trisomy 22: clinical report and review.
American journal of medical genetics 1990;36(1):7-10.
1990: D S Murthy; A S Teebi; T S Sundareshan; Shafika A Al-Awadi
Familial fragile secondary constriction on chromosome 2 (2q11) with unusual features and psychomotor retardation.
Indian journal of pediatrics 1990;57(2):257-60.
1990: Shafika A Al-Awadi; TI Farag; A S Teebi; Kamal Naguib; T S Sundareshan; D S Murthy
Down syndrome in Kuwait.
American journal of medical genetics. Supplement 1990;7():87-8.
1990: S J Abulhasan; A S Teebi; M Zaki; I Hammad; Shafika A Al-Awadi; D S Krishna Murthy
Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short stature.
Annales de génétique 1990;33(4):234-8.
1989: M H el-Badramany; TI Farag; Shafika A Al-Awadi; I M Hammad; A Abdelkader; D S Murthy
Familial manic-depressive illness with deleted short arm of chromosome 21: coincidental or causal?
The British journal of psychiatry : the journal of mental science 1989;155():856-7.
1989: Azhar Daoud; Mohamed Zaki; Qusay Al-Saleh; A S Teebi; Shafika A Al-Awadi
Congenital hypothyroidism in Kuwait.
Journal of tropical pediatrics 1989;35(6):312-4.
1989: A S Teebi; Qusay Al-Saleh; M M Hassoon; TI Farag; Shafika A Al-Awadi
Macrosomia, microphthalmia, +/- cleft palate and early infant death: a new autosomal recessive syndrome.
Clinical genetics 1989;36(3):174-7.
1989: TI Farag; Shafika A Al-Awadi; S Yassin; T A el-Kassaby; S Jaefary; R Usha; R Uma; S A Mady; M Fakhr; M Mannae
Anencephaly: a vanishing problem in Bedouins?
Journal of medical genetics 1989;26(8):538-9.
1989: A S Teebi; T S Sundareshan; M Y Hammouri; Shafika A Al-Awadi; Qusay Al-Saleh
A new autosomal recessive disorder resembling Weaver syndrome.
American journal of medical genetics 1989;33(4):479-82.
1989: Kamal Naguib; A S Teebi; TI Farag; Shafika A Al-Awadi; M Y el-Khalifa
Familial uterine hernia syndrome: report of an Arab family with four affected males.
American journal of medical genetics 1989;33(2):180-1.
1989: F M Mohammed; TI Farag; S S Gunawardana; D D al-Digashim; Shafika A Al-Awadi; S A al-Othman; T S Sundareshan
Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies.
American journal of medical genetics 1989;32(3):353-5.
1988: A S Teebi; Kamal Naguib; Shafika A Al-Awadi; Qusay Al-Saleh
New autosomal recessive faciodigitogenital syndrome.
Journal of medical genetics 1988;25(6):400-6.
1988: Kamal Naguib; T S Sundareshan; A M Bahar; Shafika A Al-Awadi; L A Jeryan; M R Hamdan
Fertility with deletion Xq25: report of three cases; possible exceptions for critical region hypothesis.
Fertility and sterility 1988;49(5):917-9.
1988: TI Farag; Shafika A Al-Awadi; S A Al-Othman; T S Sundareshan; D S Krishna Murthy; R Usha; S A Madg; R Uma
Down syndrome and trisomy 18 in the Bedouins.
American journal of medical genetics 1988;29(4):943-4.
1988: Shafika A Al-Awadi; Kamal Naguib; S A al-Othman; T S Sundareshan
Trisomy 4q: 46, xy,-11, +der (11), t(4;11) (q27; q25) pat in a child with multiple congenital anomalies.
Indian journal of pediatrics 1988;55(2):308-11.
1988: A S Teebi; Shafika A Al-Awadi; M J Marafie; R A Bushnaq; S Satyanath
Osteoporosis-pseudoglioma syndrome with congenital heart disease: a new association.
Journal of medical genetics 1988;25(1):32-6.
1988: Shafika A Al-Awadi; TI Farag; S Satyanath; T S Sundareshan
Metacarpophalangeal pattern profile analysis in partial 9pmonosomy.
American journal of medical genetics 1988;29(1):217-9.
1987: Kamal Naguib; Shafika A Al-Awadi; M J Marafie; S Y Al-Hijji
Trisomy 18 clustering in Kuwait.
Clinical genetics 1987;32(6):379-82.
1987: TI Farag; Shafika A Al-Awadi; P Tippett; M el-Sayed; T S Sundareshan; S A Al-Othman; M H el-Badramany
Unilateral true hermaphrodite with 46,XX/46,XY dispermic chimerism.
Journal of medical genetics 1987;24(12):784-6.
1987: Kamal Naguib; A S Teebi; Shafika A Al-Awadi; M J Marafie
Brachmann-de Lange syndrome in sibs.
Journal of medical genetics 1987;24(10):627-9.
1987: TI Farag; Shafika A Al-Awadi; M C Hunt; S Satyanath; M Zahran; R Usha; R Uma
A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance?
Journal of medical genetics 1987;24(10):597-601.
1987: A S Teebi; Shafika A Al-Awadi; TI Farag; Kamal Naguib; M Y el-Khalifa
Phenylketonuria in Kuwait and Arab countries.
European journal of pediatrics 1987;146(1):59-60.
1987: TI Farag; D S Krishna Murthy; Shafika A Al-Awadi; T S Sundareshan; S A Ai-Othman; S A Mady; M A Redha
Robertsonian translocation t dic (14p;22p) with regular trisomy 21: a possible interchromosomal effect?
Annales de génétique 1987;30(3):189-92.
1987: Shafika A Al-Awadi; TI Farag; Kamal Naguib; A S Teebi; M Y el-Khalifa; M J Marafie; M A Issa; E S Mahfouz
Intestinal malformations and Down's syndrome in Arabs.
Journal of the Royal Society of Medicine 1987;80(1):61-2.
1986: Shafika A Al-Awadi; Kamal Naguib; M A Moussa; TI Farag; A S Teebi; M Y el-Khalifa
The effect of consanguineous marriages on reproductive wastage.
Clinical genetics 1986;29(5):384-8.
1986: Shafika A Al-Awadi; TI Farag; R Usha; M Y el-Khalifa; T S Sundareshan; S A Al-Othman
Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].
American journal of medical genetics 1986;23(4):931-3.
1986: Shafika A Al-Awadi; Kamal Naguib; A S Teebi; T S Sundareshan
De novo partial monosomy 21 with unusual karyotype.
Jinrui idengaku zasshi. The Japanese journal of human genetics 1986;31(1):45-8.
1986: Shafika A Al-Awadi; Kamal Naguib; TI Farag; A S Teebi; A Cuschieri; S A Al-Othman; T S Sundareshan
Complex translocation involving chromosomes Y, 1, and 3 resulting in deletion of segment 3q23----q25.
Journal of medical genetics 1986;23(1):91-2.
1986: S Portoian-Shuhaiber; Shafika A Al-Awadi; TI Farag; T S Sundareshan; H R Jindal; A A Al-Rashied
Clinical findings in an Arab boy with ring (14)(mos 46,XY,r(14)/45,XY,-14).
Annales de génétique 1986;29(2):122-4.
1986: Shafika A Al-Awadi; A S Teebi; D S Krishna Murthy; G Othman; T S Sundareshan
Klinefelter's syndrome, mosaic 46,XX/46,XY/47,XXY/48,XXXY/48,XXYY: a case report.
Annales de génétique 1986;29(2):119-21.
1985: Shafika A Al-Awadi; TI Farag; A S Teebi; Kamal Naguib; M Y el-Khalifa; Y Kelani; A Al-Ansari; R N Schimke
Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected females.
American journal of medical genetics 1985;22(3):619-22.
1985: Shafika A Al-Awadi; TI Farag; M Y el-Khalifa; A G Al-Ansari
Fibrodysplasia ossificans progressiva.
Journal of the Royal Society of Medicine 1985;78(10):881-2.
1985: Shafika A Al-Awadi; M A Moussa; K K Naguib; TI Farag; A S Teebi; M el-Khalifa; L el-Dossary
Consanguinity among the Kuwaiti population.
Clinical genetics 1985;27(5):483-6.
1985: Shafika A Al-Awadi; A S Teebi; TI Farag; K M Naguib; M Y el-Khalifa
Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome.
Journal of medical genetics 1985;22(1):36-8.
1985: Shafika A Al-Awadi; A S Teebi; T S Sundareshan
Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qter.
Annales de génétique 1985;28(3):181-4.
1984: Shafika A Al-Awadi; TI Farag; A S Teebi; Kamal Naguib; M Y El-Khalifa
Anencephaly: disappearing in Kuwait?
Lancet 1984;2(8404):701-2.
1984: Shafika A Al-Awadi; T I Fårag; Kamal Naguib; M Y El-Khalifa; A Cuschieri; G Hosny; M Zahran; A G Al-Ansari
Spondyloepiphyseal dysplasia tarda with progressive arthropathy.
Journal of medical genetics 1984;21(3):193-6.
1983: Shafika A Al-Awadi; TI Farag; Kamal Naguib; A Teebi; A Cuschieri; S Al-Othman; T S Sundareshan
Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33).
Journal of medical genetics 1983;20(6):464-5.
1983: Shafika A Al-Awadi; A Cuschieri; TI Farag; Kamal Naguib; A S Teebi; S A Al-Othman; A H Bahig
Ullrich-Turner syndrome in monozygotic twins.
American journal of medical genetics 1983;15(4):537-42.