Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2–q13.3): Molecular genetics and clinical experience in 109 cases-Reference-Cited by-同舟云学术

Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2–q13.3): Molecular genetics and clinical experience in 109 cases

Published:1995-05 Issue:5 Volume:15 Page:407-417
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Wirth B.,Rudnik-Schöneborn S.,Hahnen E.,Röhrig D.,Zerres K.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

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1. Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: A variant of infantile spinal muscular atrophy

2. Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome.

3. Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis

4. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3

5. Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6

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