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Journal De Genetique Humaine|September 1, 1989
[Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year]K Chrzanowska, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 28, 2010
Pure de novo 17q25.3 micro duplication characterized by micro array CGH in a dysmorphic infant with growth retardation, developmental delay and distal arthrogryposisT Lukusa, J P FrynsJournal of Medical Genetics|March 1, 1993
Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity?D Soekarman, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndromeD Soekarman, J P FrynsGenetic Counseling (Geneva, Switzerland)|July 14, 2000
Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescenceT Lukusa, J P FrynsAmerican Journal of Medical Genetics|July 1, 1987
Apparently new autosomal recessive syndrome of mental retardation, distal limb deficiencies, oral involvement, and possible renal defectM Buttiens, J P FrynsAmerican Journal of Medical Genetics|November 1, 1986
Distal osteolysis, short stature, mental retardation, and characteristic facial appearance: delineation of an autosomal recessive subtype of essential osteolysisP Petit, J P FrynsAnnales De Genetique|January 1, 1987
Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11)J P Fryns, A KleczkowskaAnnales De Genetique|January 1, 1996
Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(Q32;Q22) in a male patientJ P Fryns, G HendrickxGenetic Counseling (Geneva, Switzerland)|July 28, 1999
Early development (5 to 48 months) in Williams syndrome. A study of 14 childrenL Plissart, J P FrynsPageof 89