168 related articles for article (PubMed ID: 8740922)
1. Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndrome.
Wieczorek D; Gillessen-Kaesbach G; Plewa S; Passarge E
Clin Genet; 1996 Feb; 49(2):98-102. PubMed ID: 8740922
[TBL] [Abstract][Full Text] [Related]
2. Microcephaly with large anterior fontanelle, generalized convulsions, micropenis, and distinct anomalies of the hands and feet. Another example of Wiedemann syndrome?
Nevin NC; Stewart FJ; Corkey CW; Bell BA
Clin Genet; 1994 Aug; 46(2):205-8. PubMed ID: 7529662
[TBL] [Abstract][Full Text] [Related]
3. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
Meinecke P
Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190
[TBL] [Abstract][Full Text] [Related]
4. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome).
Abu-Libdeh B; Fujimoto A; Ehinger M
Am J Med Genet; 1993 Feb; 45(3):358-60. PubMed ID: 8434624
[TBL] [Abstract][Full Text] [Related]
5. Smith-Lemli-Opitz syndrome: report of a new case and review of the literature.
Srsen S
Acta Paediatr Acad Sci Hung; 1972; 13(4):301-8. PubMed ID: 4664661
[No Abstract] [Full Text] [Related]
6. Absence of thumbs, A/hypoplasia of radius, hypoplasia of ulnae, retarded bone age, short stature, microcephaly, hypoplastic genitalia, and mental retardation.
Wieczorek D; Köster B; Gillessen-Kaesbach G
Am J Med Genet; 2002 Mar; 108(3):209-13. PubMed ID: 11891687
[TBL] [Abstract][Full Text] [Related]
7. Two sisters with growth failure, microcephaly, peculiar facies and apical dystrophy: the presentation of brachymorphism-onychodysplasia-dysphalangism syndrome?
Ounap K; Justus I; Lipping-Sitska M
Clin Dysmorphol; 1998 Jan; 7(1):45-50. PubMed ID: 9546830
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Acrodysplasia, severe ossification abnormalities with short stature, and fibular hypoplasia.
Castriota-Scanderbeg A; Zelante L; Masala S; Gasparini P; Lachman RS
Am J Med Genet; 1999 May; 84(1):68-73. PubMed ID: 10213049
[TBL] [Abstract][Full Text] [Related]
11. Anaesthetic implications of the child with Robinow syndrome.
Sleesman JB; Tobias JD
Paediatr Anaesth; 2003 Sep; 13(7):629-32. PubMed ID: 12950866
[TBL] [Abstract][Full Text] [Related]
12. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.
Lin HJ; Kakkis ED; Eteson DJ; Lachman RS
Am J Med Genet; 1993 Sep; 47(4):534-9. PubMed ID: 8256819
[TBL] [Abstract][Full Text] [Related]
13. Wiedemann-Steiner Syndrome With 2 Novel KMT2A Mutations.
Min Ko J; Cho JS; Yoo Y; Seo J; Choi M; Chae JH; Lee HR; Cho TJ
J Child Neurol; 2017 Feb; 32(2):237-242. PubMed ID: 27777327
[TBL] [Abstract][Full Text] [Related]
14. Aarskog syndrome in a Brazilian boy born to consanguineous parents.
Guion-Almeida ML; Richieri-Costa A
Am J Med Genet; 1992 Jul; 43(5):808-10. PubMed ID: 1642267
[TBL] [Abstract][Full Text] [Related]
15. Aarskog syndrome: report of a family with review and discussion of nosology.
Teebi AS; Rucquoi JK; Meyn MS
Am J Med Genet; 1993 Jun; 46(5):501-9. PubMed ID: 8322809
[TBL] [Abstract][Full Text] [Related]
16. Novel findings in a patient with Weaver or a Weaver-like syndrome.
Scarano G; Della Monica M; Lonardo F; Neri G
Am J Med Genet; 1996 May; 63(2):378-81. PubMed ID: 8725789
[TBL] [Abstract][Full Text] [Related]
17. Mirror image duplication of the hands and feet: report of a sporadic case with multiple congenital anomalies.
Hersh JH; Dela Cruz TV; Pietrantoni M; von Drasek-Ascher G; Turnquest MA; Yacoub OA; Joyce MR
Am J Med Genet; 1995 Nov; 59(3):341-5. PubMed ID: 8599358
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitalia.
Porteous ME; Burn J
J Med Genet; 1990 May; 27(5):339-40. PubMed ID: 2352265
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
