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Genetic Counseling (Geneva, Switzerland)
|
October 24, 2000
Hypersplenism and portal hypertension with vena porta thrombosis in cartilage-hair hypoplasia (metaphyseal chondrodysplasia, McKusick type, MIM *250250)
J P Fryns
Prenatal Diagnosis
|
January 1, 1995
Prenatal diagnosis and long survival of Fryns syndrome
J P Fryns
Journal of Medical Genetics
|
August 1, 1987
Congenital scalp defects with distal limb reduction anomalies
J P Fryns
Archives Francaises De Pediatrie
|
May 1, 1988
[Unmanageable hair syndrome associated with epilepsy, deafness and phalangeal aplasia, or William's syndrome?]
J P Fryns
Clinical Dysmorphology
|
August 5, 1998
Meier-Gorlin syndrome: the adult phenotype
J P Fryns
Journal of Medical Genetics
|
July 25, 1998
Another holoprosencephaly locus at 7q21.2?
J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
May 3, 2001
Micro-ablepharon of the upper eyelids and vaginal atresia
J P Fryns
American Journal of Medical Genetics
|
April 24, 1999
On the nosology of severe acrofacial dysostosis with limb deficiency
J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Neuroblastoma in patients with constitutional chromosomal changes
J P Fryns
American Journal of Medical Genetics
|
January 1, 1993
Dolichomegasigmoid in Aarskog syndrome
J P Fryns
Page
of 112
Search research articles
Search
Showing results (21-30 of 1,120) with videos related to
Sort By:
Page
of 112
Genetic Counseling (Geneva, Switzerland)
|
October 24, 2000
Hypersplenism and portal hypertension with vena porta thrombosis in cartilage-hair hypoplasia (metaphyseal chondrodysplasia, McKusick type, MIM *250250)
J P Fryns
Prenatal Diagnosis
|
January 1, 1995
Prenatal diagnosis and long survival of Fryns syndrome
J P Fryns
Journal of Medical Genetics
|
August 1, 1987
Congenital scalp defects with distal limb reduction anomalies
J P Fryns
Archives Francaises De Pediatrie
|
May 1, 1988
[Unmanageable hair syndrome associated with epilepsy, deafness and phalangeal aplasia, or William's syndrome?]
J P Fryns
Clinical Dysmorphology
|
August 5, 1998
Meier-Gorlin syndrome: the adult phenotype
J P Fryns
Journal of Medical Genetics
|
July 25, 1998
Another holoprosencephaly locus at 7q21.2?
J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
May 3, 2001
Micro-ablepharon of the upper eyelids and vaginal atresia
J P Fryns
American Journal of Medical Genetics
|
April 24, 1999
On the nosology of severe acrofacial dysostosis with limb deficiency
J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Neuroblastoma in patients with constitutional chromosomal changes
J P Fryns
American Journal of Medical Genetics
|
January 1, 1993
Dolichomegasigmoid in Aarskog syndrome
J P Fryns
Page
of 112