259 related articles for article (PubMed ID: 3189398)
21. 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]
22. Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies.
Verp MS; Simpson JL; Elias S; Carson SA; Sarto GE; Feingold M
Fertil Steril; 1983 Jul; 40(1):80-5. PubMed ID: 6862042
[TBL] [Abstract][Full Text] [Related]
23. [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].
Amini-Elihou S
J Genet Hum; 1970 Dec; 18(4):307-63. PubMed ID: 5524816
[No Abstract] [Full Text] [Related]
24. [The Freeman-Sheldon syndrome].
Grasshoff H; St Braun H; Sakreida M
Beitr Orthop Traumatol; 1978 May; 25(5):241-7. PubMed ID: 98163
[No Abstract] [Full Text] [Related]
25. Sandrow syndrome of mirror hands and feet and facial abnormalities.
Kogekar N; Teebi AS; Vockley J
Am J Med Genet; 1993 Apr; 46(2):126-8. PubMed ID: 8387243
[TBL] [Abstract][Full Text] [Related]
26. [Hand deformities in Freeman-Sheldon syndrome and their surgical treatment].
Martini AK; Banniza von Bazan U
Z Orthop Ihre Grenzgeb; 1983; 121(5):623-9. PubMed ID: 6649810
[TBL] [Abstract][Full Text] [Related]
27. Dominant inheritance of cleft palate with minor abnormalities of hands and feet: a new syndrome?
Kirk EP; Wilson M
Clin Dysmorphol; 1999 Jul; 8(3):193-7. PubMed ID: 10457853
[TBL] [Abstract][Full Text] [Related]
28. Autosomal dominant inheritance of scalp defects with ectrodactyly.
Bonafede RP; Beighton P
Am J Med Genet; 1979; 3(1):35-41. PubMed ID: 474617
[TBL] [Abstract][Full Text] [Related]
29. Familial recurrence of geleophysic dysplasia.
Koiffmann CP; Wajntal A; Ursich MJ; Pupo AA
Am J Med Genet; 1984 Nov; 19(3):483-6. PubMed ID: 6507494
[TBL] [Abstract][Full Text] [Related]
30. An unusual syndrome with mental retardation and sparse hair.
Nicolaides P; Baraitser M
Clin Dysmorphol; 1993 Jul; 2(3):232-6. PubMed ID: 8287185
[TBL] [Abstract][Full Text] [Related]
31. [Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome].
Szappanos L; Czeizel E; Szepesi K
Orv Hetil; 1984 Mar; 125(11):633-8. PubMed ID: 6700970
[No Abstract] [Full Text] [Related]
32. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
Martínez-Frías ML; Martín M; Pardo M; Fernandez de las Heras F; Frías JL
Am J Med Genet; 1995 Jan; 55(2):213-6. PubMed ID: 7717420
[TBL] [Abstract][Full Text] [Related]
33. Robinow syndrome: with special emphasis on dermatoglyphics and hand malformations (split hand).
Balci S; Erçal MD; Say B; Atasü M
Clin Dysmorphol; 1993 Jul; 2(3):199-207. PubMed ID: 8287181
[TBL] [Abstract][Full Text] [Related]
34. Carpenter syndrome with normal intelligence: Brazilian girl born to consanguineous parents.
Richieri-Costa A; Pirolo Júnior L; Cohen MM
Am J Med Genet; 1993 Aug; 47(2):281-3. PubMed ID: 8213921
[TBL] [Abstract][Full Text] [Related]
35. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports].
Fabbro MA; D'Agostino S; Costa L; Musi L; Cappellari F
Pediatr Med Chir; 1997; 19(2):121-4. PubMed ID: 9312747
[TBL] [Abstract][Full Text] [Related]
36. Brief clinical report: two children with de novo del(9p).
Young RS; Bader P; Palmer CG; Kaler SG; Hodes ME
Am J Med Genet; 1983 Apr; 14(4):751-7. PubMed ID: 6846405
[TBL] [Abstract][Full Text] [Related]
37. The genetics of hand malformations.
Temtamy SA; McKusick VA
Birth Defects Orig Artic Ser; 1978; 14(3):i-xviii, 1-619. PubMed ID: 215242
[No Abstract] [Full Text] [Related]
38. Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.
Tas E; Sebastian J; Madan-Khetarpal S; Sweet P; Yatsenko AN; Pollock N; Rajkovic A; Schneck FX; Yatsenko SA; Witchel SF
Am J Med Genet A; 2017 Jan; 173(1):221-224. PubMed ID: 27649277
[TBL] [Abstract][Full Text] [Related]
39. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
Gollop TR; Fontes LR
Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752
[TBL] [Abstract][Full Text] [Related]
40. Familial progressive sinoatrial and atrioventricular conduction disease of adult onset with sudden death, dilated cardiomyopathy, and brachydactyly. A new type of heart-hand syndrome?
Sinkovec M; Petrovic D; Volk M; Peterlin B
Clin Genet; 2005 Aug; 68(2):155-60. PubMed ID: 15996213
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]