Obesity (nutrition)

Citations 31-39 of 39 total displayed.

Electronic letters
DEFECT 11 syndrome associated with agenesis of the corpus callosum

TOSHIYUKI YAMAMOTO, SHINJIROU AKABOSHI, HARUAKI NINOMIYA, EIJI NANBA
J. Med. Genet. 2001; 38: e5. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Bardet-Biedl and Cohen syndromes: differential diagnostic criteria

METTE WARBURG, RUTH RIISE, PHILIP BEALES, FRANCES FLINTER
J. Med. Genet. 2000; 37: e46. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Germline mosaicism for a GNAS1 mutation and Albright hereditary osteodystrophy

MICHEALA A ALDRED, R JANE BAGSHAW, KAY MACDERMOT, DAVID CASSON, SIMON H MURCH, J A WALKER-SMITH, RICHARD C TREMBATH
J. Med. Genet. 2000; 37: e35. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Mapping of the human genes (SLC23A2 and SLC23A1) coding for vitamin C transporters 1 and 2 (SVCT1 and SVCT2) to 5q23 and 20p12, respectively

CONSTANTINE A STRATAKIS, SUSAN E TAYMANS, RUSHAD DARUWALA, JIAN SONG, MARK LEVINE
J. Med. Genet. 2000; 37: e20. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Alström syndrome: confirmation of linkage to chromosome 2p12-13 and phenotypic heterogeneity in three affected sibs

URS ZUMSTEG, PATRICK Y MULLER, ANDRÉ R MISEREZ
J. Med. Genet. 2000; 37: e8. [Extract] [Full text] [PDF] [Request Permissions]  

Short reports
Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype

Roel Hordijk, Henk Wierenga, Hans Scheffer, Beike Leegte, Robert M W Hofstra, Irene Stolte-Dijkstra
J. Med. Genet. 1999; 36: 782-785. [Abstract] [Full text] [PDF] [Request Permissions]  

Review articles
Monosomy 1p36

Anne Slavotinek, Lisa G Shaffer, Stuart K Shapira
J. Med. Genet. 1999; 36: 657-663. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes

Albert David, Pierre Bitoun, Didier Lacombe, Jean-Claude Lambert, Annie Nivelon, Jacqueline Vigneron, Alain Verloes
J. Med. Genet. 1999; 36: 599-603. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey

P L Beales, N Elcioglu, A S Woolf, D Parker, F A Flinter
J. Med. Genet. 1999; 36: 437-446. [Abstract] [Full text] [PDF] [Request Permissions]