127 related articles for article (PubMed ID: 15930908)
1. Growth deficiency in oculodigitoesophagoduodenal (Feingold) syndrome--case report and review of the literature.
Shaw-Smith C; Willatt L; Thalange N
Clin Dysmorphol; 2005 Jul; 14(3):155-158. PubMed ID: 15930908
[TBL] [Abstract][Full Text] [Related]
2. Vertebral defects in a patient with Feingold syndrome.
Kellermayer R; Weisenbach J; Gyuris P; Aszmann M; Kosztolányi G
Clin Dysmorphol; 2005 Oct; 14(4):213-214. PubMed ID: 16155427
[No Abstract] [Full Text] [Related]
3. Feingold syndrome: report of a new family and review.
Courtens W; Levi S; Verbelen F; Verloes A; Vamos E
Am J Med Genet; 1997 Nov; 73(1):55-60. PubMed ID: 9375923
[TBL] [Abstract][Full Text] [Related]
4. Familial syndromic duodenal atresia: Feingold syndrome.
Holder-Espinasse M; Ahmad Z; Hamill J; Pahari A; Misra D; Drake D; Winter RM; Wilson LC
Eur J Pediatr Surg; 2004 Apr; 14(2):112-6. PubMed ID: 15185158
[TBL] [Abstract][Full Text] [Related]
5. [Feingold syndrome].
Alessandri JL; Graber D; Tiran-Rajaofera I; Montbrun A; Pilorget H; Samperiz S; Attali T; de Napoli-Cocci S
Arch Pediatr; 2000 Jun; 7(6):637-40. PubMed ID: 10911531
[TBL] [Abstract][Full Text] [Related]
6. Imperforate anus in Feingold syndrome.
Büttiker V; Wojtulewicz J; Wilson M
Am J Med Genet; 2000 May; 92(3):166-9. PubMed ID: 10817649
[TBL] [Abstract][Full Text] [Related]
7. Expanding the phenotype of feingold syndrome-2.
Grote LE; Repnikova EA; Amudhavalli SM
Am J Med Genet A; 2015 Dec; 167A(12):3219-25. PubMed ID: 26360630
[TBL] [Abstract][Full Text] [Related]
8. Exudative retinopathy, cerebral calcifications, duodenal atresia, preaxial polydactyly, micropenis, microcephaly and short stature: a new syndrome?
Isidor B; Le Meur G; Conti C; Caldagues E; Lainey E; Launay E; Leclair MD; Le Francois T; Pichon O; Boisseau P; Migraine A; Keren B; Le Caignec C; Crow YJ; David A
Am J Med Genet A; 2013 Aug; 161A(8):1829-32. PubMed ID: 23824919
[TBL] [Abstract][Full Text] [Related]
9. A Feingold syndrome case with previously undescribed features and a new mutation.
Koçak H; Ozaydin E; Köse G; Marcelis CL; Kamsteeg EJ; Ceylaner S
Genet Couns; 2009; 20(3):261-7. PubMed ID: 19852433
[TBL] [Abstract][Full Text] [Related]
10. Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.
Brunner HG; Winter RM
J Med Genet; 1991 Jun; 28(6):389-94. PubMed ID: 1870095
[TBL] [Abstract][Full Text] [Related]
11. How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
Ravel A; Chouery E; Stora S; Jalkh N; Villard L; Temtamy S; Mégarbané A
Am J Med Genet A; 2011 Apr; 155A(4):880-4. PubMed ID: 21416592
[TBL] [Abstract][Full Text] [Related]
12. Duodenal atresia: consider Feingold syndrome.
Chopra M; James C; Adams S; Mowat D
J Paediatr Child Health; 2010 Mar; 46(3):136-7. PubMed ID: 20415994
[No Abstract] [Full Text] [Related]
13. Distal aphalangia, an extra metatarsal, short stature and microcephaly: a second case.
Di Rocco M
Clin Dysmorphol; 2002 Oct; 11(4):295-6. PubMed ID: 12401998
[TBL] [Abstract][Full Text] [Related]
14. MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome.
Frydman M; Katz M; Cabot SG; Soen G; Kauschansky A; Sirota L
Am J Med Genet; 1997 Aug; 71(3):251-7. PubMed ID: 9268091
[TBL] [Abstract][Full Text] [Related]
15. Delineation of EFTUD2 haploinsufficiency-related phenotypes through a series of 36 patients.
Lehalle D; Gordon CT; Oufadem M; Goudefroye G; Boutaud L; Alessandri JL; Baena N; Baujat G; Baumann C; Boute-Benejean O; Caumes R; Decaestecker C; Gaillard D; Goldenberg A; Gonzales M; Holder-Espinasse M; Jacquemont ML; Lacombe D; Manouvrier-Hanu S; Marlin S; Mathieu-Dramard M; Morin G; Pasquier L; Petit F; Rio M; Smigiel R; Thauvin-Robinet C; Vasiljevic A; Verloes A; Malan V; Munnich A; de Pontual L; Vekemans M; Lyonnet S; Attié-Bitach T; Amiel J
Hum Mutat; 2014 Apr; 35(4):478-85. PubMed ID: 24470203
[TBL] [Abstract][Full Text] [Related]
16. Split hand malformation, hypospadias, microphthalmia, distinctive face and short stature in two brothers suggest a new syndrome.
García-Ortiz JE; Banda-Espinoza F; Zenteno JC; Galván-Uriarte LM; Ruiz-Flores P; García-Cruz D
Am J Med Genet A; 2005 May; 135(1):21-7. PubMed ID: 15809993
[TBL] [Abstract][Full Text] [Related]
17. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
Feingold M; Hall BD; Lacassie Y; Martínez-Frías ML
Am J Med Genet; 1997 Mar; 69(3):245-9. PubMed ID: 9096752
[TBL] [Abstract][Full Text] [Related]
18. An apparently new mental retardation syndrome in three elderly sisters.
Viljoen DL; Kallis J; Voges S; Marais AS; van Vuuren I
Clin Genet; 1991 Jul; 40(1):6-11. PubMed ID: 1884519
[TBL] [Abstract][Full Text] [Related]
19. Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: a new autosomal recessive MCA/MR syndrome?
Kondoh T; Yamamoto T; Kono Y; Matsumoto T; Sugawara H; Matsumoto N; Moriuchi H
Am J Med Genet; 2001 Jul; 102(1):63-7. PubMed ID: 11471174
[TBL] [Abstract][Full Text] [Related]
20. A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features.
Vinkler C; Leshinsky-Silver E; Michelson M; Haas D; Lerman-Sagie T; Lev D
Eur J Med Genet; 2014; 57(6):288-92. PubMed ID: 24709618
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
