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American Journal of Medical Genetics|January 1, 1991
Bilateral complete polysyndactyly (type IV Haas)G Gillessen-Kaesbach, F Majewski
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
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|July 24, 2001
Adiposity indices in German children and adolescents with genetically confirmed Prader-Willi syndrome (PWS)B P Hauffa, G Schlippe, G Gillessen-Kaesbach
Clinical Genetics|February 1, 1996
Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndromeD Wieczorek, G Gillessen-Kaesbach, S Plewa, et al.
Clinical Dysmorphology|August 24, 1999
Aplasia cutis congenita--etiological relationship to antiphospholipid syndrome?C Roll, L Hanssler, T Voit, et al.
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