1468-5833 < 1468-6244 < 1469-0292

Facettes : Author.f

List of bibliographic references

Number of relevant bibliographic references: 77.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
001074 (2007)	Ineke Van Der Burgt ; William Kupsky ; Stephani Stassou ; Ali Nadroo ; Cândida Barroso ; Angelika Diem ; Christian P. Kratz ; Radovan Dvorsky ; Mohammad Reza Ahmadian ; Martin Zenker	Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation
001085 (1987)		Correction
001858 (1965)	Mieczyslaw Wender ; Jerzy Kosowicz ; Jan Steffen ; Bozena Zgorzalewicz	Familial Occurrence of Trisomy 16-18
001859 (1967)	H. Luginbühl ; S. K. Chacko ; D. F. Patterson ; W. Medway	Congenital Hereditary Lymphoedema in the Dog Part II—Pathological Studies*
001860 (1967)	D. F. Patterson ; W. Medway ; H. Luginbühl ; S. Chacko	Congenital Hereditary Lymphoedema in the Dog. Part I—Clinical and Genetic Studies*
001861 (1976)	H F Shammas ; K F Tabbara ; V M Der Kaloustian	Atypical serum cholinesterase in a family with congenital distichiasis.
001862 (1975)	G. Pescia ; P E Ferrier ; D. Wyss-Hutin ; D. Klein	45,X Turner's syndrome in monozygotic twin sisters.
001863 (1965)	Malcolm A. Ferguson-Smith	Karyotype-phenotype Correlations in Gonadal Dysgenesis and Their Bearing on the Pathogenesis of Malformations
001864 (1965)	John R. Esterly	Congenital Hereditary Lymphoedema
001865 (1992)	V. Petrovic ; S. Nasioulas ; C W Chow ; L. Voullaire ; M. Schmidt ; H. Dahl	Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies.
001866 (1992)	R V Mikelsaar ; I W Lurie	Atypical case of Aarskog syndrome.
001867 (1992)	P D Turnpenny ; J C Dean ; I A Auchterlonie ; A W Johnston	Cardiofaciocutaneous syndrome with new ectodermal manifestations.
001868 (1991)	P. Meinecke ; E. Passarge	Microcephalic osteodysplastic primordial dwarfism type I/III in sibs.
001869 (1991)	D R Mcleod ; L R Wesselman ; D I Hoar	Pallister-Killian syndrome: additional manifestations of cleft palate and sacral appendage.
001870 (1989)	M R Pinto ; R P Leite ; A. Areias	Features of Turner's and DiGeorge's syndromes in a child with an X;22 translocation.
001871 (1988)	D L Viljoen	Klippel-Trenaunay-Weber syndrome (angio-osteohypertrophy syndrome).
001872 (1987)	R F Mueller	The Alagille syndrome (arteriohepatic dysplasia).
001873 (1988)	P. Merlob ; D. Steier ; S H Reisner	Autosomal dominant isolated ('uncomplicated') microcephaly.
001874 (1987)	J E Allanson	Noonan syndrome.
001875 (1987)	R F Dale	Primary lymphoedema when found with distichiasis is of the type defined as bilateral hyperplasia by lymphography.
001876 (1986)	D A Couzin ; N. Haites ; J L Watt ; A W Johnston	Partial trisomy 7 (q32----qter) syndrome in two children.

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