285 related articles for article (PubMed ID: 6897847)
1. Computers in paediatrics. 3. Genetic counselling for autosomal dominant conditions.
Tay JS; Yip WC
J Singapore Paediatr Soc; 1982; 24(3-4):133-7. PubMed ID: 6897847
[No Abstract] [Full Text] [Related]
2. Computers in paediatrics. 2. Genetic counselling for sex linked recessive conditions.
Tay JS; Yip WC
J Singapore Paediatr Soc; 1982; 24(3-4):125-32. PubMed ID: 6897846
[No Abstract] [Full Text] [Related]
3. Penetrance of familial hypertrophic cardiomyopathy.
Charron P; Carrier L; Dubourg O; Tesson F; Desnos M; Richard P; Bonne G; Guicheney P; Hainque B; Bouhour JB; Mallet A; Feingold J; Schwartz K; Komajda M
Genet Couns; 1997; 8(2):107-14. PubMed ID: 9219008
[TBL] [Abstract][Full Text] [Related]
4. Osteochondromatosis in an isolated community in Manitoba.
Dooley J; Black B; Piper A
Arctic Med Res; 1988; 47 Suppl 1():415-9. PubMed ID: 3272654
[No Abstract] [Full Text] [Related]
5. [Genetic counseling].
Plasencia Amela A; Hernando Acero I; Benavides Benavides A; Fernández Toral L; Fernández Cuesta M
An Esp Pediatr; 1987 Aug; 27(2):130-4. PubMed ID: 3662268
[No Abstract] [Full Text] [Related]
6. Nephropathy in hereditary osteo-onycho dysplasia (HOOD): variable expression or genetic heterogeneity?
Lommen EJ; Hamel BC; te Slaa RL
Prog Clin Biol Res; 1989; 305():157-60. PubMed ID: 2762348
[No Abstract] [Full Text] [Related]
7. Genetic counseling.
Degnan M; Peters J; Porter IH; Gottesman DM
Am Fam Physician; 1975 Jul; 12(1):111-7. PubMed ID: 125534
[No Abstract] [Full Text] [Related]
8. [Clinical study and genetic 3q28 locus linkage in 2 Swiss families with Kjer dominant optic atrophy (OPA1)].
Lefèvre A; Hiroz C; Zografos L; Schorderet DF; Munier FL
Klin Monbl Augenheilkd; 1998 May; 212(5):301-4. PubMed ID: 9677562
[TBL] [Abstract][Full Text] [Related]
9. [Genic diseases and chromosome diseases].
Robert JM; Cordier MP
Soins; 1983 Apr; (403):3-6. PubMed ID: 6553367
[No Abstract] [Full Text] [Related]
10. [Genetic counseling].
Klein D
Bull Schweiz Akad Med Wiss; 1972 Sep; 28(5):250-65. PubMed ID: 4566685
[No Abstract] [Full Text] [Related]
11. [Pedigree analysis of two families with Alport's syndrome].
Wässer S; Theile H; Schöne D; Lemme B
Padiatr Grenzgeb; 1980; 19(3):167-71. PubMed ID: 7454376
[No Abstract] [Full Text] [Related]
12. [Hereditarily transmitted pathologic fragilitas ossium].
Mezhenina EP
Tsitol Genet; 1974; 8(1):20-3. PubMed ID: 4829675
[No Abstract] [Full Text] [Related]
13. Single-gene disorders.
Kirkman HN
Pediatr Ann; 1978 Jun; 7(6):54-5, 58-60, 63-4 passim. PubMed ID: 673496
[No Abstract] [Full Text] [Related]
14. Linkage studies in alcohol-responsive myoclonic dystonia.
Gasser T; Bereznai B; Müller B; Pruszak-Seel R; Damrich R; Deuschl G; Oertel WH
Mov Disord; 1996 Jul; 11(4):363-70. PubMed ID: 8813214
[TBL] [Abstract][Full Text] [Related]
15. Genetic heterogeneity of Oguchi's disease.
Singh JR
Indian J Ophthalmol; 1990; 38(4):193-4. PubMed ID: 2086477
[TBL] [Abstract][Full Text] [Related]
16. [Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree].
De Marchi S; Proto G; Jengo A; Collinassi P; Basile A
Minerva Med; 1983 Feb; 74(7):301-6. PubMed ID: 6828258
[TBL] [Abstract][Full Text] [Related]
17. A high incidence of PKD in a large geographic area of south-western Hungary: a medical genetic study.
Forrai G; Tauszik T; Tauszik N; Mohr T; Tunyogi MC; Holics C; Bánkövi G; Gál I
Prog Clin Biol Res; 1989; 305():89-94. PubMed ID: 2762359
[No Abstract] [Full Text] [Related]
18. [Hypo-/aplasia of the nasal bones--an autosomal dominant inherited anomaly].
Ernst M; Schilbach U
HNO; 1987 Nov; 35(11):478-81. PubMed ID: 3692934
[TBL] [Abstract][Full Text] [Related]
19. Hereditary hemorrhagic telangiectasia with juvenile polyposis--coincidence or linked autosomal dominant inheritance?
Ballauff A; Koletzko S
Z Gastroenterol; 1999 May; 37(5):385-8. PubMed ID: 10413846
[TBL] [Abstract][Full Text] [Related]
20. Familial comedones. Evidence for autosomal dominant inheritance.
Cantú JM; Gómez-Bustamente MO; González-Mendoza A; Sánchez-Corona J
Arch Dermatol; 1978 Dec; 114(12):1807-9. PubMed ID: 153732
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
