Langer-Giedion syndrome with del 8 (q24.13-q24.22).
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 40, doi. 10.1111/j.1399-0004.1987.tb03321.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1987 AND VI 32 AND IP 1
Results: 16
1
2
Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 66, doi. 10.1111/j.1399-0004.1987.tb03326.x
- By:
- Publication type:
- Article
3
Carrier detection of haemophilia A using DNA markers in families with an isolated affected male.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 10, doi. 10.1111/j.1399-0004.1987.tb03316.x
- By:
- Publication type:
- Article
4
Proximal duplication of the long arm of chromosome 10 (10q11.2 → 10q22): a distinct clinical entity.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 61, doi. 10.1111/j.1399-0004.1987.tb03325.x
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- Publication type:
- Article
5
Non-mosaic isodicentric X-chromosome in a patient with secondary amenorrhea.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 20, doi. 10.1111/j.1399-0004.1987.tb03317.x
- By:
- Publication type:
- Article
6
Tetrasomy for the short arm of chromosome 12 with accessory isochromosome (+i(12p)) and a marked LDH-B gene dosage effect.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 1, doi. 10.1111/j.1399-0004.1987.tb03314.x
- By:
- Publication type:
- Article
7
Predicting intellectual functioning in 47,XXY boys from characteristics of sibs.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 24, doi. 10.1111/j.1399-0004.1987.tb03318.x
- By:
- Publication type:
- Article
8
Familial transmission of a ring chromosome 21.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 35, doi. 10.1111/j.1399-0004.1987.tb03320.x
- By:
- Publication type:
- Article
9
Parental age, and how extra isochromosomes (secondary trisomy) arise.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 75, doi. 10.1111/j.1399-0004.1987.tb03328.x
- By:
- Publication type:
- Article
10
Multiple pterygium syndrome: a case complicated by malignant hyperthermia.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 5, doi. 10.1111/j.1399-0004.1987.tb03315.x
- By:
- Publication type:
- Article
11
Tandem duplication (1) (q11 → q22) in a male infant with multiple congenital malformations.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 46, doi. 10.1111/j.1399-0004.1987.tb03322.x
- By:
- Publication type:
- Article
12
Robertsonian translocation and an extra microchromosome: aetiology and effect on meiotic segregation.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 57, doi. 10.1111/j.1399-0004.1987.tb03324.x
- By:
- Publication type:
- Article
13
An aminopterin-like syndrome without aminopterin (ASSAS).
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 28, doi. 10.1111/j.1399-0004.1987.tb03319.x
- By:
- Publication type:
- Article
14
18ph+ is a normal chromosomal variant.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 79, doi. 10.1111/j.1399-0004.1987.tb03329.x
- By:
- Publication type:
- Article
15
Genetic history: I. The Schneersons of Lubavich.
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 70, doi. 10.1111/j.1399-0004.1987.tb03327.x
- By:
- Publication type:
- Article
16
Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5)(p13.1 → p15.3).
- Published in:
- Clinical Genetics, 1987, v. 32, n. 1, p. 49, doi. 10.1111/j.1399-0004.1987.tb03323.x
- By:
- Publication type:
- Article