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Genetic 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 arthrogryposis
T Lukusa, J P Fryns
Human Genetics
|
January 1, 1983
Two pericentric inversions inv(7)(p15;q32) and inv(9)(p11;q13) in a male with absence of vas deferens
P Petit, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
April 29, 1998
Trisomy 21 in a second trimester male hydropic fetus with "Noonan-syndrome-phenotype": nuchal and thoracic lymphangiomatosis, oedema of the dorsum of hands and feet, and bicuspid pulmonary valve
J P Fryns, P Moerman
American Journal of Medical Genetics
|
September 19, 1997
Precocious puberty in Klinefelter syndrome: non-specific result of neurological deficit?
J P Fryns, K Devriendt
Journal of Medical Genetics
|
October 1, 1988
Mucosal neuromata syndrome (MEN type IIb (III))
J P Fryns, K Chrzanowska
American Journal of Human Genetics
|
January 1, 1983
Expression of fragile site at 10q25 in normal culture conditions
P Petit, J P Fryns
Journal 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 Fryns
Prenatal Diagnosis
|
October 1, 1996
Multiple-marker screen positive results in Rubinstein-Taybi syndrome
J P Fryns, P Ramaekers
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome
D Soekarman, J P Fryns
American Journal of Medical Genetics
|
September 6, 1996
Velo-facio-skeletal syndrome versus Aarskog syndrome
J P Fryns, K Devriendt
Page
of 112
Search research articles
Search
Showing results (71-80 of 1,120) with videos related to
Sort By:
Page
of 112
Genetic 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 arthrogryposis
T Lukusa, J P Fryns
Human Genetics
|
January 1, 1983
Two pericentric inversions inv(7)(p15;q32) and inv(9)(p11;q13) in a male with absence of vas deferens
P Petit, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
April 29, 1998
Trisomy 21 in a second trimester male hydropic fetus with "Noonan-syndrome-phenotype": nuchal and thoracic lymphangiomatosis, oedema of the dorsum of hands and feet, and bicuspid pulmonary valve
J P Fryns, P Moerman
American Journal of Medical Genetics
|
September 19, 1997
Precocious puberty in Klinefelter syndrome: non-specific result of neurological deficit?
J P Fryns, K Devriendt
Journal of Medical Genetics
|
October 1, 1988
Mucosal neuromata syndrome (MEN type IIb (III))
J P Fryns, K Chrzanowska
American Journal of Human Genetics
|
January 1, 1983
Expression of fragile site at 10q25 in normal culture conditions
P Petit, J P Fryns
Journal 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 Fryns
Prenatal Diagnosis
|
October 1, 1996
Multiple-marker screen positive results in Rubinstein-Taybi syndrome
J P Fryns, P Ramaekers
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1992
Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome
D Soekarman, J P Fryns
American Journal of Medical Genetics
|
September 6, 1996
Velo-facio-skeletal syndrome versus Aarskog syndrome
J P Fryns, K Devriendt
Page
of 112