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Journal of Medical Genetics
|
June 1, 1997
Lethal femoral-facial syndrome: a case with unusual manifestations
Y Gillerot, C Fourneau, T Willems, et al.
Prenatal Diagnosis
|
August 19, 1999
Prenatal ultrasound detection of congenital cataract in trisomy 21
M Romain, J Awoust, C Dugauquier, et al.
Clinical Genetics
|
May 1, 1990
Trisomy 20q. A new case and further phenotypic delineation
C Herens, A Verloes, F Laloux, et al.
American Journal of Medical Genetics
|
October 1, 1990
Mental retardation, short stature, almond-shaped eyes, small downturned mouth and coned epiphyses: a new case of Hunter-Fraser syndrome
L Van Maldergem, Y Gillerot, N Perlmutter, et al.
Pediatric Radiology
|
January 1, 1990
Lethal short-rib with median cleft and without polydactyly: a fourth case
L van Maldergem, Y Gillerot, E Salmin, et al.
Clinical Genetics
|
November 1, 1990
Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance
L Van Maldergem, Y Gillerot, M Godhaird, et al.
American Journal of Medical Genetics
|
January 15, 1992
Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome)
A Verloes, Y Gillerot, E Walczak, et al.
Acta Clinica Belgica
|
January 1, 1990
Bradycardia in a case of type II glycogenosis (Pompe's disease) revealing in early neonatal period
L Van Maldergem, D Haumont, D Saurty, et al.
Clinical Genetics
|
January 1, 1992
Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?
L van Maldergem, C Wetzburger, A Verloes, et al.
American Journal of Medical Genetics
|
May 15, 1993
Oral-facial-digital syndrome type I in a newborn male
Y Gillerot, M Heimann, C Fourneau, et al.
Page
of 12
Search research articles
Search
Showing results (11-20 of 114) with videos related to
Sort By:
Page
of 12
Journal of Medical Genetics
|
June 1, 1997
Lethal femoral-facial syndrome: a case with unusual manifestations
Y Gillerot, C Fourneau, T Willems, et al.
Prenatal Diagnosis
|
August 19, 1999
Prenatal ultrasound detection of congenital cataract in trisomy 21
M Romain, J Awoust, C Dugauquier, et al.
Clinical Genetics
|
May 1, 1990
Trisomy 20q. A new case and further phenotypic delineation
C Herens, A Verloes, F Laloux, et al.
American Journal of Medical Genetics
|
October 1, 1990
Mental retardation, short stature, almond-shaped eyes, small downturned mouth and coned epiphyses: a new case of Hunter-Fraser syndrome
L Van Maldergem, Y Gillerot, N Perlmutter, et al.
Pediatric Radiology
|
January 1, 1990
Lethal short-rib with median cleft and without polydactyly: a fourth case
L van Maldergem, Y Gillerot, E Salmin, et al.
Clinical Genetics
|
November 1, 1990
Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance
L Van Maldergem, Y Gillerot, M Godhaird, et al.
American Journal of Medical Genetics
|
January 15, 1992
Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome)
A Verloes, Y Gillerot, E Walczak, et al.
Acta Clinica Belgica
|
January 1, 1990
Bradycardia in a case of type II glycogenosis (Pompe's disease) revealing in early neonatal period
L Van Maldergem, D Haumont, D Saurty, et al.
Clinical Genetics
|
January 1, 1992
Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?
L van Maldergem, C Wetzburger, A Verloes, et al.
American Journal of Medical Genetics
|
May 15, 1993
Oral-facial-digital syndrome type I in a newborn male
Y Gillerot, M Heimann, C Fourneau, et al.
Page
of 12