Survey of amniocentesis for fetal sex determination in hemophilia carriers.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 337, doi. 10.1111/j.1399-0004.1976.tb00058.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1976 AND VI 10 AND IP 5
Results: 16
1
2
Further evidence'for the autosomal-recessive inheritance of the COFS syndrome.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 343, doi. 10.1111/j.1399-0004.1976.tb00059.x
- By:
- Publication type:
- Article
3
Aberrant axillary breast tissue: A report of a family with six affected women in two generations.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 325, doi. 10.1111/j.1399-0004.1976.tb00056.x
- By:
- Publication type:
- Article
4
A cytogenetic survey of 14,069 newborn infants: II. Preliminary clinical findings on children with sex chromosome anomalies.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 285, doi. 10.1111/j.1399-0004.1976.tb00050.x
- By:
- Publication type:
- Article
5
Hypertrichosis lanuginosa in a mother and son.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 303, doi. 10.1111/j.1399-0004.1976.tb00052.x
- By:
- Publication type:
- Article
6
A methodology for establishing a diagnostic index for syndromes of unknown etiology.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 249, doi. 10.1111/j.1399-0004.1976.tb00045.x
- By:
- Publication type:
- Article
7
Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomalies.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 307, doi. 10.1111/j.1399-0004.1976.tb00053.x
- By:
- Publication type:
- Article
8
Sanfilippo B disease in two related sibships. Biochemical studies in patients, parents and sibs.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 273, doi. 10.1111/j.1399-0004.1976.tb00048.x
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- Publication type:
- Article
9
The frequency of PKU and hyperphenylalaninemia in Sweden - a study in institutions for the mentally retarded as well as in neonates.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 313, doi. 10.1111/j.1399-0004.1976.tb00054.x
- By:
- Publication type:
- Article
10
Structural aberrations of the long arm of chromosome no. 22: Report of a family with translocation t(11;22) (q25;q11).
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 329, doi. 10.1111/j.1399-0004.1976.tb00057.x
- By:
- Publication type:
- Article
11
True hermaphroditism with XX/XY sex chromosome mosaicism: Report of a case.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 265, doi. 10.1111/j.1399-0004.1976.tb00047.x
- By:
- Publication type:
- Article
12
Prenatal diagnosis of fucosidosis.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 260, doi. 10.1111/j.1399-0004.1976.tb00046.x
- By:
- Publication type:
- Article
13
Clinical variability in Sanfilippo B disease: a report on six patients in two related sibships.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 279, doi. 10.1111/j.1399-0004.1976.tb00049.x
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- Publication type:
- Article
14
Addendum.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 297, doi. 10.1111/j.1399-0004.1976.tb00051.x
- Publication type:
- Article
15
ABSTRACTS.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 348, doi. 10.1111/j.1399-0004.1976.tb00060.x
- Publication type:
- Article
16
Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1.
- Published in:
- Clinical Genetics, 1976, v. 10, n. 5, p. 319, doi. 10.1111/j.1399-0004.1976.tb00055.x
- By:
- Publication type:
- Article