X-linked recessive combined pituitary hormone deficiency is mapped to Xp22.3-Xp11 in a Chinese family.

[1]  T. Ogata,et al.  Mutation and gene copy number analyses of six pituitary transcription factor genes in 71 patients with combined pituitary hormone deficiency: identification of a single patient with LHX4 deletion. , 2010, The Journal of clinical endocrinology and metabolism.

[2]  M. Dattani,et al.  Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD) , 2009, Clinical endocrinology.

[3]  M. Dattani,et al.  Hypopituitarism Oddities: Congenital Causes , 2007, Hormone Research in Paediatrics.

[4]  L. Notarangelo,et al.  X-linked hypogammaglobulinemia and isolated growth hormone deficiency: an update , 2007, Immunologic research.

[5]  Brenda J. Crowe,et al.  Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency , 2006, Journal of Medical Genetics.

[6]  L. Notarangelo,et al.  Update on X-linked hypogammaglobulinemia with isolated growth hormone deficiency , 2005, Current opinion in allergy and clinical immunology.

[7]  M. Dattani Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter? , 2005, Clinical endocrinology.

[8]  R. Lovell-Badge,et al.  Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism. , 2005, American journal of human genetics.

[9]  P. Thomas,et al.  Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency. , 2002, American journal of human genetics.

[10]  P. Thomas,et al.  Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism. , 2002, Genomics.

[11]  T. Ogata,et al.  SHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal features. , 2002, The Journal of clinical endocrinology and metabolism.

[12]  E. Mariman,et al.  Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes. , 2000, Genomics.

[13]  M. Raynaud,et al.  X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one family. , 1998, American journal of medical genetics.

[14]  A. Rosenthal,et al.  Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome , 1997, Nature Genetics.

[15]  U. Landegren,et al.  X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26. , 1997, American journal of human genetics.

[16]  E. Mariman,et al.  Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings. , 1996, American journal of medical genetics.

[17]  F. Wondisford,et al.  A Mutation in the POU-Homeodomain of Pit-1 Responsible for Combined Pituitary Hormone Deficiency , 1992, Science.

[18]  J. Puck,et al.  Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiency. , 1991, The Journal of pediatrics.

[19]  D. Dunger,et al.  Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia. , 2001, Human molecular genetics.