Literature DB >> 14231762

[FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?].

H R WIEDEMANN.   

Abstract

Entities:  

Keywords:  ABNORMALITIES; CHILD; CLITORIS; GENETICS, HUMAN; HYPERTROPHY; INFANT, NEWBORN; INFANT, PREMATURE, DISEASES; PROGNATHISM; TONGUE; UMBILICAL HERNIA

Mesh：

Year:  1964        PMID： 14231762

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  76 in total

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2.  Wilms' tumor and adrenocortical carcinoma with hemihypertrophy and hamartomas.

Authors:  S Müller; H Gadner; B Weber; M Vogel; H Riehm
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3.  Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells.

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Authors:  Y Stefan; C Bordi; S Grasso; L Orci
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5.  Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome.

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6.  Raised somatomedin associated with normal growth hormone. A cause of Beckwith-Wiedemann syndrome?

Authors:  G S Spencer; F Schabel; H Frisch
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7.  Pancreatoblastoma in a neonate with Wiedemann-Beckwith syndrome.

Authors:  T H Koh; J E Cooper; C L Newman; T M Walker; E M Kiely; E B Hoffmann
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8.  Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases.

Authors:  A L Kosseff; J Herrmann; E F Gilbert; C Viseskul; M Lubinsky; J M Opitz
Journal:  Eur J Pediatr       Date:  1976-10-01       Impact factor: 3.183

9.  Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.

Authors:  R A Spritz; D Mager; R M Pauli; R Laxova
Journal:  Am J Hum Genet       Date:  1986-08       Impact factor: 11.025

10.  Molecular analysis of patients with Wiedemann-Beckwith syndrome. I. Gene dosage on the short arm of chromosome 11.

Authors:  A Nyström; W Engström; J Cheetham; P N Schofield
Journal:  Eur J Pediatr       Date:  1992-07       Impact factor: 3.183
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