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K Devriendt

Showing results (11-20 of 230) with videos related to

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Journal of Medical Genetics|March 1, 1996
Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndromeK Devriendt, L D'Espallier, J P Fryns
American Journal of Medical Genetics|March 1, 1996
Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?K Devriendt, E Legius, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 geneJ P Fryns, M D'Hooghe, K Devriendt
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Lumbosacral spina bifida and myeloschizis in a female foetus with de novo X/autosomal translocation (t(X;22)(q27;q121))J P Fryns, K Devriendt, P Moerman
Clinical Dysmorphology|July 1, 1997
Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum: an example of the variable clinical spectrum of the Acrocallosal syndrome?J P Fryns, K Devriendt, E Legius
Tijdschrift Voor Psychiatrie|October 9, 2010
[Sleep disturbances in Smith-Magenis syndrome: treatment with melatonin and beta-adrenergic antagonists]A Van Thillo, K Devriendt, D Willekens
Clinical Genetics|July 11, 1998
Deletion in chromosome region 22q11 in a child with CHARGE associationK Devriendt, A Swillen, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Unilateral limb reduction defect and lumbar appendage: disorganisation-like syndrome?K Devriendt, L Vandenbossche, J P Fryns
American Journal of Medical Genetics|June 22, 1999
Follow-up of an adult with Keutel syndromeK Devriendt, M Holvoet, J P Fryns
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Further delineation of the KBG syndromeK Devriendt, M Holvoet, J P Fryns
Pageof 23

Showing results (11-20 of 230) with videos related to

Sort By:
Pageof 23
Journal of Medical Genetics|March 1, 1996
Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndromeK Devriendt, L D'Espallier, J P Fryns
American Journal of Medical Genetics|March 1, 1996
Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?K Devriendt, E Legius, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 geneJ P Fryns, M D'Hooghe, K Devriendt
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Lumbosacral spina bifida and myeloschizis in a female foetus with de novo X/autosomal translocation (t(X;22)(q27;q121))J P Fryns, K Devriendt, P Moerman
Clinical Dysmorphology|July 1, 1997
Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum: an example of the variable clinical spectrum of the Acrocallosal syndrome?J P Fryns, K Devriendt, E Legius
Tijdschrift Voor Psychiatrie|October 9, 2010
[Sleep disturbances in Smith-Magenis syndrome: treatment with melatonin and beta-adrenergic antagonists]A Van Thillo, K Devriendt, D Willekens
Clinical Genetics|July 11, 1998
Deletion in chromosome region 22q11 in a child with CHARGE associationK Devriendt, A Swillen, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Unilateral limb reduction defect and lumbar appendage: disorganisation-like syndrome?K Devriendt, L Vandenbossche, J P Fryns
American Journal of Medical Genetics|June 22, 1999
Follow-up of an adult with Keutel syndromeK Devriendt, M Holvoet, J P Fryns
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Further delineation of the KBG syndromeK Devriendt, M Holvoet, J P Fryns
Pageof 23