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G Gillessen-Kaesbach

Showing results (1-10 of 83) with videos related to

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Birth Defects Original Article Series|January 1, 1996
Familial holoprosencephaly: further example of autosomal recessive inheritanceG Gillessen-Kaesbach
American Journal of Medical Genetics|January 1, 1991
Bilateral complete polysyndactyly (type IV Haas)G Gillessen-Kaesbach, F Majewski
American Journal of Medical Genetics|December 22, 1999
Trisomy 13 with bilateral hand oligodactylyB Kuschel, G Gillessen-Kaesbach
Journal of Medical Genetics|March 1, 1994
Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotypeG Gillessen-Kaesbach, B Horsthemke
Clinical Dysmorphology|October 25, 2000
Multiple subcutaneous granular-cell tumours in a patient with Noonan syndromeD R Lohmann, G Gillessen-Kaesbach
Prenatal Diagnosis|October 1, 1990
Ring 19 mosaicism detected during prenatal diagnosisG Gillessen-Kaesbach, N T Ngo
Neuropediatrics|December 7, 2007
Investigation of recessive ataxia loci in patients with young age of onsetC Zühlke, V Bernard, G Gillessen-Kaesbach
American Journal of Medical Genetics|May 3, 1996
Jeune syndrome with tongue lobulation and preaxial polydactyly, and Jeune syndrome with situs inversus and asplenia: compound heterozygosity Jeune-Mohr and Jeune-Ivemark?E Majewski, B Oztürk, G Gillessen-Kaesbach
Clinical Genetics|July 1, 1997
Cardio-facio-cutaneous (CFC) syndrome--a distinct entity? Report of three patients demonstrating the diagnostic difficulties in delineation of CFC syndromeD Wieczorek, F Majewski, G Gillessen-Kaesbach
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
A nine-month-old boy with microcephaly, cataracts, intracerebral calcifications and dysmorphic signs: an additional observation of an autosomal recessive congenital infection-like syndrome?D Wieczorek, G Gillessen-Kaesbach, E Passarge
Pageof 9

Showing results (1-10 of 83) with videos related to

Sort By:
Pageof 9
Birth Defects Original Article Series|January 1, 1996
Familial holoprosencephaly: further example of autosomal recessive inheritanceG Gillessen-Kaesbach
American Journal of Medical Genetics|January 1, 1991
Bilateral complete polysyndactyly (type IV Haas)G Gillessen-Kaesbach, F Majewski
American Journal of Medical Genetics|December 22, 1999
Trisomy 13 with bilateral hand oligodactylyB Kuschel, G Gillessen-Kaesbach
Journal of Medical Genetics|March 1, 1994
Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotypeG Gillessen-Kaesbach, B Horsthemke
Clinical Dysmorphology|October 25, 2000
Multiple subcutaneous granular-cell tumours in a patient with Noonan syndromeD R Lohmann, G Gillessen-Kaesbach
Prenatal Diagnosis|October 1, 1990
Ring 19 mosaicism detected during prenatal diagnosisG Gillessen-Kaesbach, N T Ngo
Neuropediatrics|December 7, 2007
Investigation of recessive ataxia loci in patients with young age of onsetC Zühlke, V Bernard, G Gillessen-Kaesbach
American Journal of Medical Genetics|May 3, 1996
Jeune syndrome with tongue lobulation and preaxial polydactyly, and Jeune syndrome with situs inversus and asplenia: compound heterozygosity Jeune-Mohr and Jeune-Ivemark?E Majewski, B Oztürk, G Gillessen-Kaesbach
Clinical Genetics|July 1, 1997
Cardio-facio-cutaneous (CFC) syndrome--a distinct entity? Report of three patients demonstrating the diagnostic difficulties in delineation of CFC syndromeD Wieczorek, F Majewski, G Gillessen-Kaesbach
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
A nine-month-old boy with microcephaly, cataracts, intracerebral calcifications and dysmorphic signs: an additional observation of an autosomal recessive congenital infection-like syndrome?D Wieczorek, G Gillessen-Kaesbach, E Passarge
Pageof 9