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Jill Northup

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Jill K Northup; Judy C Hawkins; Lillian H Lockhart; Reuben Matalon; Gopalrao Velagaleti
A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.
Neena L Champaigne; Nicole A Laird; Jill K Northup; Gopalrao Velagaleti
Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3-month-old with severe pediatric gastroesophageal reflux.
Jill K Northup; Kären E Wain; Judy C Hawkins; Reuben Matalon; Gopalrao Velagaleti
First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficiencies.

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All Publications

2011: Jill K Northup; Judy C Hawkins; Lillian H Lockhart; Reuben Matalon; Gopalrao Velagaleti
A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.
European journal of medical genetics 2011;54(4):e394-8.
2009: Neena L Champaigne; Nicole A Laird; Jill K Northup; Gopalrao Velagaleti
Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3-month-old with severe pediatric gastroesophageal reflux.
American journal of medical genetics. Part A 2009;149A(4):751-4.
2008: Jill K Northup; Kären E Wain; Judy C Hawkins; Reuben Matalon; Gopalrao Velagaleti
First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficiencies.
American journal of medical genetics. Part A 2008;146A(19):2578-82.
2008: Susanna L Cooke; Jill K Northup; Neena L Champaige; William Zinser; Paul A W Edwards; Lillian H Lockhart; Gopalrao Velagaleti
Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement.
American journal of medical genetics. Part A 2008;146A(9):1166-72.
2008: Karmaine Millington; S David Hudnall; Jill K Northup; Neli I Panova; Gopalrao Velagaleti
Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: report of 2 new cases.
Experimental and molecular pathology 2008;84(2):189-93.
2007: S David Hudnall; Jill K Northup; Neli I Panova; Kauser Suleman; Gopalrao Velagaleti
Prolonged preleukemic phase of chronic myelogenous leukemia.
Experimental and molecular pathology 2007;83(3):484-9.
2007: Jill K Northup; Kathleen Griffis; Judy Hawkins; Lillian H Lockhart; Gopalrao Velagaleti
Unusual pseudo dicentric, psu dic (1;19)(q10;q13.42), in a female with premature ovarian failure.
Fertility and sterility 2007;87(3):697.e5-8.
2007: Jill K Northup; Swarupa A Gadre; Yimin Ge; Lillian H Lockhart; Gopalrao Velagaleti
Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?
European journal of haematology 2007;78(2):152-6.
2007: Zhiqin Wang; Gopalrao Velagaleti; Mahmoud A Eltorky; Wendell W Tang; Hal K Hawkins; Elizabeth A Jones; Jill K Northup; Neli I Panova; Suimin Qiu
Cytogenetic and molecular studies of an unusual case of multiple primary alveolar rhabdomyosarcomas: low-level chromosomal instability and reciprocal translocation t(6;11).
Experimental and molecular pathology 2007;82(1):58-62.
2005: Vijay S Tonk; Golder N Wilson; Svetlana A Yatsenko; Pawel Stankiewicz; James R Lupski; Robert C Schutt; Jill K Northup; Gopalrao Velagaleti
Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype.
American journal of medical genetics. Part A 2005;139A(2):136-40.
2005: Gabriel A Bien-Willner; Pawel Stankiewicz; James R Lupski; Jill K Northup; Gopalrao Velagaleti
Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosis.
American journal of hematology 2005;79(4):309-13.
2005: Gopalrao Velagaleti; Gabriel A Bien-Willner; Jill K Northup; Lillian H Lockhart; Judy C Hawkins; Syed M Jalal; Marjorie Withers; James R Lupski; Pawel Stankiewicz
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.
American journal of human genetics 2005;76(4):652-62.