[侏儒症-特殊面容-发育迟缓，皮特型，皮特-罗杰斯-丹克斯综合征，沃尔夫-赫希霍恩综合征，4p缺失综合征] - Suppr

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[Dwarfism-dysmorphic facies-retardation, Pitt type, Pitt-Rogers-Danks syndrome, Wolf-Hirschhorn syndrome, 4p-syndrome].

作者信息

Ishikiriyama S

机构信息

Division of Medical Genetics, Chiba Children's Hospital.

出版信息

Ryoikibetsu Shokogun Shirizu. 2001(33):584-5.

PMID:11462581

Abstract

摘要

相似文献

[Dwarfism-dysmorphic facies-retardation, Pitt type, Pitt-Rogers-Danks syndrome, Wolf-Hirschhorn syndrome, 4p-syndrome].

Ryoikibetsu Shokogun Shirizu. 2001(33):584-5.

Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotype.

Am J Med Genet. 1996 Dec 2;66(1):104-12. doi: 10.1002/(SICI)1096-8628(19961202)66:1<104::AID-AJMG28>3.0.CO;2-V.

Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.

Am J Med Genet. 1996 Dec 2;66(1):95-100. doi: 10.1002/(SICI)1096-8628(19961202)66:1<95::AID-AJMG26>3.0.CO;2-K.

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.

J Med Genet. 1997 Jul;34(7):569-72. doi: 10.1136/jmg.34.7.569.

A girl with the Pitt-Rogers-Danks syndrome.

Am J Med Genet. 1989 Jan;32(1):140-1. doi: 10.1002/ajmg.1320320130.

Wolf-Hirschhorn (4P-) syndrome in adults.

Genet Couns. 2001;12(1):35-48.

[Familial Pitt-Rogers-Danks: two new cases].

Rev Neurol. 2001;33(5):439-43.

A further patient with the Pitt-Rogers-Danks syndrome of mental retardation, unusual face, and intrauterine growth retardation.

Am J Med Genet. 1986 May;24(1):29-32. doi: 10.1002/ajmg.1320240105.

From Pitt-Rogers-Danks syndrome to Wolf-Hirschhorn syndrome and back?

Am J Med Genet. 1996 Dec 2;66(1):113-5. doi: 10.1002/(SICI)1096-8628(19961202)66:1<113::AID-AJMG29>3.0.CO;2-U.

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome.

Am J Med Genet. 1996 Dec 2;66(1):101-3. doi: 10.1002/(SICI)1096-8628(19961202)66:1<101::AID-AJMG27>3.0.CO;2-V.

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相似文献

[Dwarfism-dysmorphic facies-retardation, Pitt type, Pitt-Rogers-Danks syndrome, Wolf-Hirschhorn syndrome, 4p-syndrome].

Ryoikibetsu Shokogun Shirizu. 2001(33):584-5.

Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotype.

Am J Med Genet. 1996 Dec 2;66(1):104-12. doi: 10.1002/(SICI)1096-8628(19961202)66:1<104::AID-AJMG28>3.0.CO;2-V.

Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.

Am J Med Genet. 1996 Dec 2;66(1):95-100. doi: 10.1002/(SICI)1096-8628(19961202)66:1<95::AID-AJMG26>3.0.CO;2-K.

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.

J Med Genet. 1997 Jul;34(7):569-72. doi: 10.1136/jmg.34.7.569.

A girl with the Pitt-Rogers-Danks syndrome.

Am J Med Genet. 1989 Jan;32(1):140-1. doi: 10.1002/ajmg.1320320130.

Wolf-Hirschhorn (4P-) syndrome in adults.

Genet Couns. 2001;12(1):35-48.

[Familial Pitt-Rogers-Danks: two new cases].

Rev Neurol. 2001;33(5):439-43.

A further patient with the Pitt-Rogers-Danks syndrome of mental retardation, unusual face, and intrauterine growth retardation.

Am J Med Genet. 1986 May;24(1):29-32. doi: 10.1002/ajmg.1320240105.

From Pitt-Rogers-Danks syndrome to Wolf-Hirschhorn syndrome and back?

Am J Med Genet. 1996 Dec 2;66(1):113-5. doi: 10.1002/(SICI)1096-8628(19961202)66:1<113::AID-AJMG29>3.0.CO;2-U.

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome.

Am J Med Genet. 1996 Dec 2;66(1):101-3. doi: 10.1002/(SICI)1096-8628(19961202)66:1<101::AID-AJMG27>3.0.CO;2-V.