137 related articles for article (PubMed ID: 2118195)
1. The cryptophthalmos syndrome.
Erdener A; Mevsim A; Ulman I; Numanoglu I
J Pak Med Assoc; 1990 Jun; 40(6):138-9. PubMed ID: 2118195
[No Abstract] [Full Text] [Related]
2. PHACE syndrome associated with club foot and thumb-in-palm deformity.
Lee SH; Kim JH; Lee JH; Kim SC
J Dermatol; 2012 Dec; 39(12):1054-5. PubMed ID: 22671438
[No Abstract] [Full Text] [Related]
3. An infant with multiple joint contractures.
Hou JW
Acta Paediatr Taiwan; 2001; 42(2):67-8. PubMed ID: 11355065
[No Abstract] [Full Text] [Related]
4. Tibial hemimelia-split hand/foot syndrome with rare anomalies.
Managoli SS; Chaturvedi P
Indian Pediatr; 2005 Feb; 42(2):190-1. PubMed ID: 15767725
[No Abstract] [Full Text] [Related]
5. Congenital cleft hand and cleft foot.
Patond KR; Kumar N; Srivastava SK
Indian Pediatr; 1991 May; 28(5):549-51. PubMed ID: 1752684
[No Abstract] [Full Text] [Related]
6. Kaufman oculocerebrofacial syndrome in a girl of 15 years.
Briscioli V; Manoukian S; Selicorni A; Livini E; Lalatta F
Am J Med Genet; 1995 Jul; 58(1):21-3. PubMed ID: 7573151
[TBL] [Abstract][Full Text] [Related]
7. A newborn diagnosed with van Maldergem syndrome.
Ulubas Isik D; Unal S; Erol S; Arslan Z; Bas AY; Demirel N
Clin Dysmorphol; 2018 Apr; 27(2):63-65. PubMed ID: 29505454
[No Abstract] [Full Text] [Related]
8. Symbrachydactyly involving hands and feet.
De Smet L; Fabry G; Fryns JP
Genet Couns; 1998; 9(1):23-7. PubMed ID: 9555583
[TBL] [Abstract][Full Text] [Related]
9. Oromandibular limb hypogenesis syndrome.
Manalo PD; Herbosa BG
J Philipp Dent Assoc; 1995; 47(2):29-33. PubMed ID: 9462075
[TBL] [Abstract][Full Text] [Related]
10. Craniosynostosis with Marfan syndrome, hand and foot anomalies.
Shah AM; Chattopadhyay A; Kher A; Bharucha BA; Karapurkar AP
Clin Dysmorphol; 1996 Jul; 5(3):263-6. PubMed ID: 8818457
[TBL] [Abstract][Full Text] [Related]
11. Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome.
Hosoki K; Ohta T; Fujita K; Nishigaki S; Shiomi M; Niikawa N; Saitoh S
Pediatr Int; 2012 Jun; 54(3):e22-5. PubMed ID: 22631585
[No Abstract] [Full Text] [Related]
12. Newly recognized ectrodactyly/deafness syndrome.
Raas-Rothschild A; Aviram A; Ben-Ami T; Berger I; Katznelson MB; Goodman RM
J Craniofac Genet Dev Biol; 1989; 9(2):121-7. PubMed ID: 2794002
[TBL] [Abstract][Full Text] [Related]
13. [The Tel Hashomer camptodactyly syndrome].
Rogovina EG; Aver'ianov IuN; Nechkina NP; Logunova LV
Zh Nevrol Psikhiatr Im S S Korsakova; 1995; 95(4):83-6. PubMed ID: 8533519
[TBL] [Abstract][Full Text] [Related]
14. Ocular involvement in proteus syndrome.
Walton DS; Muralidhar R; Ankita B; Vijayalakshmi P; Kumar SM
J Pediatr Ophthalmol Strabismus; 2013; 50(6):384. PubMed ID: 24296972
[No Abstract] [Full Text] [Related]
15. [Hand-foot-genital syndrome].
Mitsubuchi H; Endo F
Nihon Rinsho; 2006 Jun; Suppl 2():647-8. PubMed ID: 16817484
[No Abstract] [Full Text] [Related]
16. Skeletal malformations and polycystic kidney disease.
Winter RM
J Med Genet; 1993 Nov; 30(11):973. PubMed ID: 8301661
[No Abstract] [Full Text] [Related]
17. [Townes-Brocks syndrome. Case report and review of the literature].
Kotzot D; Lorenz P; Bieber A; Gröbe H
Monatsschr Kinderheilkd; 1992 Jun; 140(6):343-5. PubMed ID: 1640945
[TBL] [Abstract][Full Text] [Related]
18. Case study of an oculodentodigital (Meyer-Schwickerath) syndrome.
Ferencz M; Salacz G
Ophthalmologica; 2000; 214(5):373. PubMed ID: 10965255
[No Abstract] [Full Text] [Related]
19. Hand-foot-genital syndrome - analysis of two cases.
Piazza MJ; Urbanetz AA
JBRA Assist Reprod; 2018 Jun; 22(2):157-159. PubMed ID: 29638102
[TBL] [Abstract][Full Text] [Related]
20. Terminal 2q37 deletion and autistic behaviour.
Lukusa T; Smeets E; Vogels A; Vermeesch JR; Fryns JP
Genet Couns; 2005; 16(2):179-80. PubMed ID: 16080299
[No Abstract] [Full Text] [Related]
[Next] [New Search]