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Impact of nonmyeloablative conditioning regimens on the occurrence of pure red cell aplasia after ABO-incompatible allogeneic haematopoietic stem cell transplantation

Vox Sanguinis, 2007, Vol.92 (1), p.85-89

2007

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Dissociation of circadian activity and singing behavior from gene expression rhythms in the hypothalamus, song control nuclei and cerebellum in diurnal zebra finches

Chronobiology International, 2019, Vol.36 (9), p.1268-1284

2019

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Expanding the phenotype associated with 17q12 duplication: Case report and review of the literature

American Journal of Medical Genetics Part A, 2013, Vol.161A (2), p.352-359

2013

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Health Care Providers' Perspectives on Low HPV Vaccine Uptake and Adherence in Appalachian Kentucky

Public Health Nursing, 2013, Vol.30 (4), p.351-360

2013

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Autosomal dominant inheritance of cardiac valves anomalies in two families: Extended spectrum of left-ventricular outflow tract obstruction

American Journal of Medical Genetics Part A, 2009, Vol.149A (2), p.216-225

2009

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Complex autism spectrum disorder in a patient with a 17q12 microduplication

American Journal of Medical Genetics Part A, 2012, Vol.158A (5), p.1170-1177

2012

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XX male sex reversal with genital abnormalities associated with a de novo SOX3 gene duplication

American Journal of Medical Genetics Part A, 2012, Vol.158A (7), p.1759-1764

2012

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p.His165Pro: A novel SOX9 missense mutation of campomelic dysplasia

Journal of Obstetrics and Gynaecology Research, 2013, Vol.39 (5), p.1085-1091

2013

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From VACTERL-H to heterotaxy: Variable expressivity of ZIC3-related disorders

American Journal of Medical Genetics Part A, 2011, Vol.155A (5), p.1123-1128

2011

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Bilateral lambdoid and sagittal synostosis (BLSS): A unique craniosynostosis syndrome or predictable craniofacial phenotype?

American Journal of Medical Genetics Part A, 2009, Vol.149A (5), p.1024-1032

2009

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Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly

American Journal of Medical Genetics Part A, 2008, Vol.146A (22), p.2905-2910

2008

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Trisomy 9 mosaicism and XX sex reversal

American Journal of Medical Genetics Part A, 2007, Vol.143A (22), p.2688-2691

2007

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Resistant pure red cell aplasia after allogeneic stem cell transplantation with major ABO mismatch treated by escalating dose donor leukocyte infusion

European Journal of Haematology, 2004, Vol.73 (6), p.441-446

2004

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Megalourethra: A report of three cases associated with maternal diabetes and a review of the literature-is sonic hedgehog the common pathway?

American Journal of Medical Genetics Part A, 2005, Vol.132A (3), p.314-317

2005

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Congenital arhinia with de novo reciprocal translocation, t(3;12)(q13.2;p11.2)

American Journal of Medical Genetics Part A, 2004, Vol.130A (2), p.200-203

Hou, Jia-Woei

2004

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Mutational analysis of the luteinizing hormone receptor gene in two individuals with Leydig cell tumors

American Journal of Medical Genetics, 2002, Vol.108 (2), p.148-152

2002

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Acrania: an autopsy case and review of the literature

Congenital Anomalies, 2000, Vol.40 (1), p.40-45

2000

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Impact of nonmyeloablative conditioning regimens on the occurrence of pure red cell aplasia after ABO-incompatible allogeneic haematopoietic stem cell transplantation

Dissociation of circadian activity and singing behavior from gene expression rhythms in the hypothalamus, song control nuclei and cerebellum in diurnal zebra finches

Expanding the phenotype associated with 17q12 duplication: Case report and review of the literature

Health Care Providers' Perspectives on Low HPV Vaccine Uptake and Adherence in Appalachian Kentucky

Autosomal dominant inheritance of cardiac valves anomalies in two families: Extended spectrum of left-ventricular outflow tract obstruction

Complex autism spectrum disorder in a patient with a 17q12 microduplication

XX male sex reversal with genital abnormalities associated with a de novo SOX3 gene duplication

p.His165Pro: A novel SOX9 missense mutation of campomelic dysplasia

From VACTERL-H to heterotaxy: Variable expressivity of ZIC3-related disorders

Bilateral lambdoid and sagittal synostosis (BLSS): A unique craniosynostosis syndrome or predictable craniofacial phenotype?

Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly

Trisomy 9 mosaicism and XX sex reversal

Resistant pure red cell aplasia after allogeneic stem cell transplantation with major ABO mismatch treated by escalating dose donor leukocyte infusion

Megalourethra: A report of three cases associated with maternal diabetes and a review of the literature-is sonic hedgehog the common pathway?

Congenital arhinia with de novo reciprocal translocation, t(3;12)(q13.2;p11.2)

Mutational analysis of the luteinizing hormone receptor gene in two individuals with Leydig cell tumors

Acrania: an autopsy case and review of the literature

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